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HRID 54240作成日:2026年10月26日

Hydrochloric Acid → 3-Hydroxy-3-(2,5-dichlorophenyl)-1-butene

https://huagongshe.com/reaction/54240

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Diethyl EtherHCID 3283—
反応物TetrahydrofuranHCID 8028—
反応物Ethanone, 1-(2,5-dichlorophenyl)-HCID 75587—
反応物HCID 178418507HCID 178418507—
生成物3-Hydroxy-3-(2,5-dichlorophenyl)-1-buteneHCID 21467993—

反応手順

Under a nitrogen atmosphere, a stirred solution of 6.9 grams (0.053 mole) of vinylmagnesium bromide in 50 mL of tetrahydrofuran is cooled to 10°-15° C., and 10.0 grams (0.053 mole) of 2,5-dichloroacetophenone is added dropwise during a 20 minute period. Upon completion of addition the reaction mixture temperature is maintained at 10°-15° C. for two hours. After this time the reaction mixture is poured into 100 mL of cold aqueous 10% hydrochloric acid solution. The mixture is shaken with 100 mL of diethyl ether, and the organic layer is separated. The aqueous layer is extracted with two 50 mL portions of diethyl ether. The combined organic layers are washed with one 50 mL portion of aqueous 5% hydrochloric acid solution and then with two 30 mL portions of an aqueous solution saturated with sodium chloride. The organic layer is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 12.3 grams of 3-hydroxy-3-(2,5-dichlorophenyl)-1-butene. The NMR spectrum is consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622954
出典データセットuspto-grants-1997_04
ORD IDord-63aef65abf7044a2bacc21fdb712a96c
出典メモuspto-grants-1997_04